HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241070Generated: October 31, 2026
Acetone → 4-[(2-Amino-5-bromopyridin-3-yl)sulfinyl]-2-methylbutan-2-ol
https://huagongshe.com/reaction/241070
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetone | HCID 180 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium peroxymonosulphate | HCID 10313463 | — |
| Reactant | HCID 66820470 | HCID 66820470 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-[(2-Amino-5-bromopyridin-3-yl)sulfinyl]-2-methylbutan-2-ol | HCID 66820591 | 60% |
Reaction Steps
To a solution of 4-[(2-amino-5-bromopyridin-3-yl)thio]-2-methylbutan-2-ol (83 mg, 0.28 mmol) in a mixture of methanol (750 μL), acetone (750 μL) and water (450 μL) was added potassium peroxymonosulfate (131 mg, 0.21 mmol) and the reaction mixture was stirred for 90 minutes at 0° C. The reaction mixture was partitioned between water (20 mL) and ethyl acetate (50 mL). The organic layer was separated and washed with water (20 mL) and brine (20 mL), dried over sodium sulfate, filtered and concentrated. Purification by flash chromatography (35% to 80% ethyl acetate in hexane) gave 4-[(2-amino-5-bromopyridin-3-yl)sulfinyl]-2-methylbutan-2-ol (52 mg, 60%); MS (EI) for C10H15BrN2O2S: 308 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08648066B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-562c0c0b70344e33823acd6ef6af8784 |
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| Source note | uspto-grants-2014_02 |
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